List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 9 by Genome-Nilou Lab

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_194248.3(OTOF):c.711-49A>C	rs6547079	0.64250
NM_194248.3(OTOF):c.2736G>C (p.Leu912=)	rs4335905	0.56927
NM_194248.3(OTOF):c.509+39A>T	rs7575020	0.51850
NM_194248.3(OTOF):c.244C>T (p.Arg82Cys)	rs13031859	0.35740
NM_194248.3(OTOF):c.510-39C>T	rs884390	0.30697
NM_194248.3(OTOF):c.372A>G (p.Thr124=)	rs11687696	0.23539
NM_194248.3(OTOF):c.2580C>G (p.Val860=)	rs2272069
NM_194248.3(OTOF):c.62C>T (p.Ala21Val)	rs2148144145

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.